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CAS 1075719-78-6

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3,4-Dibromophenylboronic acid,pinacol ester

Description:
3,4-Dibromophenylboronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group and a pinacol ester moiety. This compound features a phenyl ring substituted with two bromine atoms at the 3 and 4 positions, which enhances its reactivity and potential applications in organic synthesis. The boronic acid functionality allows for participation in various reactions, such as Suzuki coupling, making it valuable in the formation of carbon-carbon bonds. The pinacol ester serves to stabilize the boronic acid group, improving its handling and storage properties. Typically, this compound is a white to off-white solid, and it is soluble in organic solvents like dichloromethane and ethyl acetate. Its reactivity and functionalization capabilities make it useful in the synthesis of complex organic molecules, particularly in medicinal chemistry and materials science. As with many organoboron compounds, care should be taken when handling due to potential reactivity and toxicity.
Formula:C12H15BBr2O2
Synonyms:
  • 3,4-Dibromophenylboronic acid,pinacol ester
  • 1,3,2-Dioxaborolane, 2-(3,4-dibromophenyl)-4,4,5,5-tetramethyl-
  • 2-(3,4-Dibromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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